Last Posted: Jan 03, 2019
- Estimating the burden and economic impact of pediatric genetic disease.
Gonzaludo Nina et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Dec - Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.
Cai Meiying et al. Medicine 2018 Dec 97(50) e13617 - January is National Birth Defects Prevention Month
CDC, January 2019 - 2019 Digital Toolkit: NATIONAL BIRTH DEFECTS PREVENTION MONTH
- National Birth Defects Prevention Month
- [Fragile X syndrome: new therapeutic strategies].
Zeidler S et al. Tijdschrift voor psychiatrie 60(5) 338-342 - Challenges in prenatal screening and counselling for fragile X syndrome.
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Parchem Jacqueline G et al. Prenatal diagnosis 2018 38(2) 140-147 - Genotyping single-sperm cells by universal MARSALA enables the acquisition of linkage information for combined pre-implantation genetic diagnosis and genome screening.
Wu Haitao et al. Journal of assisted reproduction and genetics 2018 Jun 35(6) 1071-1078 - Reflections on a Prenatal Diagnosis of Trisomy 21 Syndrome.
Davis Amanda et al. JAMA pediatrics 2017 171(3) 216
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